# Radiation Products Design,Inc - Inspection Records

Source: https://www.globalkeysolutions.net/companies/radiation-products-designinc/bf052072-9353-43aa-a28a-712fe41c9c96

> Inspection records and compliance data for Radiation Products Design,Inc in Albertville, Minnesota. Access full analysis and detailed observations.

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## Details

- Name: Radiation Products Design,Inc
- FEI Number: 2182762
- City: Albertville
- State: Minnesota
- Country Name: United States
- Address Line 1: 5218 Barthel Industrial Dr Ne
- Zip Code: 55301

## Related Documents

- [FDA Inspection 1306546 - Radiation Products Design,Inc - 2026-03-04](https://www.globalkeysolutions.net/records/fda_inspections/radiation-products-designinc/3fa6fc04-e069-44ac-b563-a45fa58fc033) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 4, 2026
- [FDA Inspection 1306546 - Radiation Products Design,Inc - 2026-03-04](https://www.globalkeysolutions.net/records/fda_inspections/radiation-products-designinc/3d1b629b-9af0-4c66-a818-c0ef2ad0090f) — classification: No Action Indicated (NAI), source: FDA, date: March 4, 2026
- [FDA Inspection 1306546 - Radiation Products Design,Inc - 2026-03-04](https://www.globalkeysolutions.net/records/fda_inspections/radiation-products-designinc/5f08b979-57a4-42e8-b243-73f932f3a60e) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 4, 2026
- [FDA Inspection 1306546 - Radiation Products Design,Inc - 2026-03-04](https://www.globalkeysolutions.net/records/fda_inspections/radiation-products-designinc/01aa4eb4-2560-437d-81d6-14166bdc6b78) — classification: No Action Indicated (NAI), source: FDA, date: March 4, 2026
- [FDA Inspection 1049026 - Radiation Products Design,Inc - 2018-04-10](https://www.globalkeysolutions.net/records/fda_inspections/radiation-products-designinc/427c5d79-300d-4dc4-b130-6f6df35eb834) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 10, 2018
- [FDA Inspection 1049026 - Radiation Products Design,Inc - 2018-04-10](https://www.globalkeysolutions.net/records/fda_inspections/radiation-products-designinc/8dcad872-8af7-4e06-929a-f104c52d1228) — classification: No Action Indicated (NAI), source: FDA, date: April 10, 2018
- [FDA Inspection 807050 - Radiation Products Design,Inc - 2012-11-06](https://www.globalkeysolutions.net/records/fda_inspections/radiation-products-designinc/c0aea88c-c9fb-4c90-a5c0-0721b80ead17) — classification: No Action Indicated (NAI), source: FDA, date: November 6, 2012
- [FDA Inspection 653205 - Radiation Products Design,Inc - 2010-03-19](https://www.globalkeysolutions.net/records/fda_inspections/radiation-products-designinc/8fcd62ed-4fc5-4ca4-8ce8-b5fa459411f3) — classification: No Action Indicated (NAI), source: FDA, date: March 19, 2010

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